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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2005-4-27
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pubmed:abstractText |
Alpha-synuclein is phosphorylated at serine 129 (Ser129) in intracellular protein aggregates called Lewy bodies. These inclusion bodies are the characteristic pathologic lesions of Parkinson disease. Here we define the role of phosphorylation of Ser129 in alpha-synuclein toxicity and inclusion formation using a Drosophila model of Parkinson disease. Mutation of Ser129 to alanine to prevent phosphorylation completely suppresses dopaminergic neuronal loss produced by expression of human alpha-synuclein. In contrast, altering Ser129 to the negatively charged residue aspartate, to mimic phosphorylation, significantly enhances alpha-synuclein toxicity. The G protein-coupled receptor kinase 2 (Gprk2) phosphorylates Ser129 in vivo and enhances alpha-synuclein toxicity. Blocking phosphorylation at Ser129 substantially increases aggregate formation. Thus Ser129 phosphorylation status is crucial in mediating alpha-synuclein neurotoxicity and inclusion formation. Because increased number of inclusion bodies correlates with reduced toxicity, inclusion bodies may protect neurons from alpha-synuclein toxicity.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Aspartic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP-Dependent Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/G-Protein-Coupled Receptor Kinase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Gprk2 protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Serine,
http://linkedlifedata.com/resource/pubmed/chemical/Synucleins,
http://linkedlifedata.com/resource/pubmed/chemical/alpha-Synuclein,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Adrenergic Receptor Kinases
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1097-6256
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
657-63
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15834418-Amino Acid Substitution,
pubmed-meshheading:15834418-Animals,
pubmed-meshheading:15834418-Animals, Genetically Modified,
pubmed-meshheading:15834418-Aspartic Acid,
pubmed-meshheading:15834418-Brain,
pubmed-meshheading:15834418-Central Nervous System,
pubmed-meshheading:15834418-Cyclic AMP-Dependent Protein Kinases,
pubmed-meshheading:15834418-Disease Models, Animal,
pubmed-meshheading:15834418-Dopamine,
pubmed-meshheading:15834418-Drosophila,
pubmed-meshheading:15834418-Drosophila Proteins,
pubmed-meshheading:15834418-G-Protein-Coupled Receptor Kinase 2,
pubmed-meshheading:15834418-Inclusion Bodies,
pubmed-meshheading:15834418-Nerve Degeneration,
pubmed-meshheading:15834418-Nerve Tissue Proteins,
pubmed-meshheading:15834418-Neurons,
pubmed-meshheading:15834418-Parkinson Disease,
pubmed-meshheading:15834418-Phosphorylation,
pubmed-meshheading:15834418-Point Mutation,
pubmed-meshheading:15834418-Retina,
pubmed-meshheading:15834418-Serine,
pubmed-meshheading:15834418-Synucleins,
pubmed-meshheading:15834418-alpha-Synuclein,
pubmed-meshheading:15834418-beta-Adrenergic Receptor Kinases
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pubmed:year |
2005
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pubmed:articleTitle |
Alpha-synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease.
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pubmed:affiliation |
Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, N.I.H., Extramural
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